Imaging and Genetic Investigation of Learning and Decision Making
NCT ID: NCT01950377
Last Updated: 2022-01-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
78 participants
OBSERVATIONAL
2014-02-11
2020-03-05
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
\- Previous research has shown that dopamine, a brain chemical, is involved in decision making. Different genes influence how much dopamine people have in their brains and how that affects their behavior. Researchers will study if genes associated with dopamine affect decision making and impulsiveness. All participants will take tests; some will have brain images taken. Researchers will study the test responses and images; they will look for how differences in these genes affect different types of decision making.
Objectives:
\- To see if genes involved in a brain chemical, dopamine, are related to impulsiveness on behavioral tests.
Eligibility:
\- Healthy adults ages 18 to 55.
Design:
* Participants will be screened with a medical history and physical exam.
* All participants in this study will have at least 1 outpatient visit to the NIH Clinical Center. Each visit will last 2 4 hours. At the first visit:
* A blood sample will be taken only from participants that have not been previously enrolled in 95-M-0150
* Participants will be given tests of their memory, attention, concentration, and thinking.
* Some participants will have a second visit. It will be scheduled as soon as possible after the first. At the second visit:
* Participants will have an MRI (magnetic resonance imaging). They will have to lie in a scanner for up to 2 hours. The MRI uses magnets, radio waves, and computers to produce detailed pictures of the brain.
* Participants will repeat the tests from the first visit. Some will be done during the MRI.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Dopamine Receptor Imaging in Mood Disorders
NCT00116077
Dopaminergic Mechanisms Underlying Human Social Behavior
NCT04205994
Study of Brain Control of Movement
NCT00017979
Measuring Brain Activity of School Age Children
NCT03407729
Neurobehavioral Mechanisms of Emotion Regulation in Depression Across the Adult Lifespan
NCT03207503
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Healthy Adults
Healthy adults healthy adults - male and female
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* are between 18 and 55 years of age
* are in good physical health
* speak English well enough to understand task instructions clearly
Exclusion Criteria
* have a major medical (e.g. heart disease), neurological (e.g. stroke) or psychiatric (e.g. bipolar disorder) illness
* have a vision and/or hearing problem that interferes with testing
* currently use any psychotropic medication, antidepressants, steroids or opiates
* currently use alcohol in excess of 14 drinks/week for males or 7 drinks/week for females.
* have a lifetime history of or currently have alcohol or substance use or dependence (excluding nicotine) that requires independent, concurrent treatment intervention (such as, antabuse or opiate treatment). This does not include self-help group treatment/intervention.
* cannot understand the consent and procedures or cannot consent themselves to the study
* Smoke more than a half pack of cigarettes a day
* NIMH employees and staff and their immediate family members will be excluded from the study per NIMH policy.
* Female subjects who are pregnant or have a positive pregnancy test 24 hours prior to an experiment will be excluded from neuroimaging studies.
* All subjects will be questioned prior to MRI scanning for possible occupational exposure to metal slivers or shavings, which may have become accidentally lodged in the tissues of the head or neck. Subjects with surgical clips or shrapnel in or near the brain or blood vessels, subjects with cochlear implants, subjects with any metallic body in the eye or CNS, and subjects with any form of implant wire or metal device which may concentrate radiofrequency fields will be excluded from MRI scanning experiments because of possible risks during MRI scanning. Those whose history is suggestive of such a problem will also be excluded from the MRI portion of the experiments. They may still participate in the behavioral experiments.
* Subjects unable to lie flat on their back for up to 2 hours or who are uncomfortable in small close spaces (have claustrophobia) will not be eligible to participate in MRI scans.
18 Years
50 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute of Mental Health (NIMH)
NIH
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Bruno B Averbeck, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
National Institute of Mental Health (NIMH)
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
NIH Clinical Center Detailed Web Page
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13-M-0190
Identifier Type: -
Identifier Source: secondary_id
130190
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.